Primary Responsibilities Include:

• Identify, establish, and maintain collaborative relationships with key opinion leaders, investigators, and institutions within academic, clinical, and health care organizations in a defined territory
• Implement KOL field strategy, KOL identification, speaker development, and support
• Leadership role in medical education for healthcare professionals through proactive communication of scientific data as well as scientific exchange of information during routine interactions
• High quality presentations of scientific data to health care professionals in various settings, including advisory boards, investigator meetings, and other appropriate venues to enhance product / disease state knowledge
• Provide on-site support to clinical operations for investigators in ongoing clinical trials, investigator-initiated studies, and registries consistent with company objectives and regulations
• Visit potential sites to assess their capabilities with regard to conduct these various forms of clinical research
• Provide professional medical affairs representation and support at global, national and regional scientific meetings, including but not limited to staffing medical affairs booths, gathering competitive intelligence, and partnering with medical information to develop post-conference scientific materials
• Develop and maintain clinical expertise in Duchenne muscular dystrophy through review of scientific journals, recent data disclosures and participation in scientific congresses
• Demonstrate an understanding of key medical and commercial strategies and provide medical support for commercial activities.

Desired Education and Skills:

• MD, PhD, PharmD, or NP/PA preferred
• 5+ years of MSL experience a plus
• Familiarity with and track record of complying with industry and regulatory compliance guidelines
• Demonstrated ability to work independently and in collaborative team environment
• Existing Neurology / Pediatric experience and relationships is a plus, experience in immunology and/or gene therapy a plus.
• Willingness to travel >50% of time
• Experience and expertise in clinical trial design, interpretation of scientific data, competitive intelligence tools, drug information systems, and medical marketing strategies
• High integrity, sense of urgency, ability to recognize time sensitivity
• Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills

This position is remote. However, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.